Anti-stem cell factor antibodies and methods of use thereof

ABSTRACT

The disclosure relates to antibodies and antigen-binding fragments thereof that bind to Stem Cell Factor (SCF). The antibodies and antigen-binding fragments thereof specifically bind to SCF248. The disclosure further relates to methods for making the antibodies, and to methods of use of the antibodies including methods of treatment for inflammatory and/or fibrotic diseases and disorders.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional of U.S. application Ser. No.17/022,465, filed Sep. 16, 2020, which claims the benefit of priority toU.S. Provisional Application No. 62/900,927, filed on Sep. 16, 2019. Thecontents of each of the aforementioned documents are incorporated byreference herein in their entireties.

FIELD

The present invention relates to antibodies and antigen-bindingfragments thereof that bind to Stem Cell Factor (SCF) and particularportions thereof, and to methods of using such antibodies andantigen-binding fragments.

REFERENCE TO AN ELECTRONIC SEQUENCE LISTING

The contents of the electronic sequence listing(OPSL_001_04US_SeqList_ST26.xml; Size: 65,334 bytes; and Date ofCreation: Sep. 2, 2022) is herein incorporated by reference in itsentirety.

BACKGROUND

Inflammatory diseases are a major cause of morbidity and mortalityworldwide. Some types of chronic inflammation can lead to fibrosis,which is the formation or development of excess fibrous connectivetissue in an organ or tissue as a reparative or reactive process, asopposed to formation of fibrous tissue as a normal constituent of anorgan or tissue. Chronic inflammation as well as fibrosis can affectnearly all tissues and organ systems, and fibrotic tissue remodeling caninfluence cancer metastasis and accelerate chronic graft rejection intransplant recipients.

Stem cell factor (SCF) and its receptor c-Kit are important factors ofthe perpetuation of chronic inflammation and in fibrotic diseases(El-Koraie, et al., Kidney Int. 60: 167 (2001); Powell, et al., Am. J.Physiol. 289: G2 (2005); El Kossi, et al., Am. J. Kidney Dis. 41: 785(2003); Powell, et al., Am. J. Physiol. 277: C183 (1999) Ding et al JPathol. 2013 June; 230(2):205-14, Berlin et al Lab Invest. 2006 June;86(6):557-65, Rasky et al Am J Physiol Lung Cell Mol Physiol. 2020 Jan.1; 318(1):L200-L211). c-Kit is a type III receptor-tyrosine kinase thatis present in many cell types (Orr-Urtreger et al., Development 109: 911(1990). Immune cells such as mast cells, eosinophils, and innatelymphoid cells 2 and 3 (ILC2 and ILC3) are all c-Kit+ cells that maydrive the chronic inflammatory process, depending on the disease andorgan involved. Upon initiation of an inflammatory response, variousmediators, including SCF, activate c-Kit+ immune cells, which in turnproduce cytokines that cause fibroblasts to become activatedmyofibroblasts. Myofibroblasts secrete extracellular matrix proteins,collagen, and fibronectin, resulting in fibrosis of tissue. Activatedmyofibroblasts, activated epithelia, endothelia, macrophages,eosinophils, mast cells, monocytes, and other cells also express SCF onthe cell surface, which activates more c-Kit+ immune cells, resulting inmore cytokine release and perpetuating the inflammation.

There is a need in the art for more efficient and more specifictreatments for inflammatory diseases. The present disclosure addressesthis and other needs.

SUMMARY OF THE DISCLOSURE

In one aspect, the present disclosure provides antibodies and fragmentsthereof that specifically bind to stem cell factor (SCF). In someembodiments, the antibodies and fragments thereof specifically bind tothe SCF isoform SCF248. In some embodiments, the antibodies andfragments thereof comprise heavy chain complementarity determiningregions (CDRs), wherein heavy chain CDR1 CDR2, and CDR3 comprise SEQ IDNOs: 1, 2, and 3, respectively. In some embodiments, the antibodies andfragments thereof comprise light chain CDRs, wherein the light chainCDR1 CDR2, and CDR3 comprise SEQ ID NOs: 4, 5, and 6, respectively. Insome embodiments, the antibodies and fragments thereof comprise heavychain CDR1, CDR2, and CDR3 comprising SEQ ID NOs: 1, 37, and 3,respectively. In some embodiments, the antibodies and fragments thereofcomprise a heavy chain variable region comprising at least 80%, at least85%, at least 90%, at least 95%, or at least 99% identity to a sequenceselected from the group consisting of SEQ ID NOs: 7, 8, 9, 10, 11, and12. In some embodiments, the antibodies and fragments thereof comprise alight chain variable region comprising at least 80%, at least 85%, atleast 90%, at least 95%, or at least 99% identity to a sequence selectedfrom the group consisting of SEQ ID NOs: 13, 14, 15, 16, and 17. In someembodiments, the antibodies and fragments thereof comprise a heavy chainvariable region comprising an amino acid sequence selected from thegroup consisting of SEQ ID NOs: 7, 8, 9, 10, 11, and 12, and a lightchain variable region comprising an amino acid sequence selected fromthe group consisting of SEQ ID NOs: 13, 14, 15, 16, and 17.

In some embodiments, the antibody or fragment thereof comprises a heavychain variable region amino acid sequence according to SEQ ID NO: 7 anda light chain variable region amino acid sequence according to SEQ IDNO: 16. In some embodiments, the antibody or fragment thereof of claim1, wherein the antibody or fragment thereof comprises a heavy chainvariable region amino acid sequence according to SEQ ID NO: 8 and alight chain variable region amino acid sequence according to SEQ ID NO:16. In some embodiments, the antibody or fragment thereof comprises aheavy chain variable region amino acid sequence according to SEQ ID NO:9 and a light chain variable region amino acid sequence according to SEQID NO: 16. In some embodiments, the antibody or fragment thereofcomprises a heavy chain variable region amino acid sequence according toSEQ ID NO: 10 and a light chain variable region amino acid sequenceaccording to SEQ ID NO: 16. In some embodiments, the antibody orfragment thereof comprises a heavy chain variable region amino acidsequence according to SEQ ID NO: 11 and a light chain variable regionamino acid sequence according to SEQ ID NO: 16. In some embodiments, theantibody or fragment thereof comprises a heavy chain variable regionamino acid sequence according to SEQ ID NO: 12 and a light chainvariable region amino acid sequence according to SEQ ID NO: 16.

In some embodiments, the antibody or fragment thereof is humanized. Insome embodiments, the antibody is a monoclonal antibody. In someembodiments, the antibody comprises a human IgG1 domain or a human IgG4domain. In some embodiments, the antibody is an antigen bindingfragment, wherein the fragment is selected from a Fab, F(ab′)2, Fab′,scFv, and single domain antibody (sdAb).

In some embodiments, the antibody or fragment thereof blocks theinteraction between SCF (e.g. SCF248) and c-Kit. In some embodiments,the antibody specifically binds to SCF248. In some embodiments, theantibody does not bind to SCF220. In some embodiments, the antibodyprevents the interaction of SCF248 and c-kit by causing theinternalization of SCF, making it unavailable on the cell surface.

In one aspect, the present disclosure provides pharmaceuticalcompositions comprising the antibody or fragment thereof providedherein. In some embodiments, the pharmaceutical composition comprises apharmaceutically acceptable carrier, diluent or excipient.

In some embodiments, the present disclosure provides isolated nucleicacid molecules encoding the antibody or fragment thereof providedherein. In some embodiments, the present disclosure provides anexpression vector comprising the nucleic acid encoding the antibody orfragment thereof. In some embodiments, the present disclosure provides arecombinant host cell comprising the expression vector.

In one aspect, the present disclosure provides methods for making anantibody that specifically binds to stem cell factor isoform 248(SCF248), the method comprising immunizing a host animal with a peptidecomprising SEQ ID NO: 30 (ASSLRNDSSSSNRKAKNPPGD) or a fragment thereof,and obtaining an antibody from the immunized host animal. In someembodiments, the host animal is not a human. In some embodiments, thefragment of SEQ ID NO: 30 comprises at least 5, at least 6, at least 7,at least 8, at least 9, at least 10, at least 11, at least 12, at least13, at least 14, at least 15, at least 16, at least 17, at least 18, atleast 19, or 20 contiguous amino acids of SEQ ID NO: 30. In someembodiments, the fragment of SEQ ID NO: 30 comprises 5, 6, 7, 8, 9, 10,11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 contiguous amino acids of SEQID NO: 30. In some embodiments, the N-terminal amino acid of thefragment of SEQ ID NO: 30 is the alanine at position 1 at the N-terminusof SEQ ID NO: 30. In some embodiments, the method comprises immunizingthe host animal with a peptide consisting of SEQ ID NO: 30. In someembodiments, the antibody from the immunized host animal is obtainedfrom an immune cell isolated from the host animal. In some embodiments,the method further comprises generating a hybridoma using the immunecell. Thus, in some embodiments, the present disclosure provideshybridomas that produce monoclonal antibodies described herein.

In one aspect, the present disclosure provides an antibody or fragmentthereof that specifically binds to SCF248, wherein the antibody orfragment thereof binds to an epitope comprising at least 8, at least 9,at least 10, at least 11, at least 12, or at least 13 contiguous aminoacids of SEQ ID NO: 33, wherein the antibody inhibits the interaction ofSCF248 with c-Kit. In further embodiments, the epitope comprises SEQ IDNO: 33 or SEQ ID NO: 36. In yet further embodiments, the epitopeconsists of SEQ ID NO: 33 or SEQ ID NO: 36.

In one aspect, the present disclosure provides compositions and methodsfor inhibiting the interaction between SCF and c-Kit. C-kit is expressedon immune cells, hematopoietic stem cells, and some structural cells.C-kit's ligand SCF248 can be upregulated on myofibroblasts, activatedepithelia, endothelia, macrophages, eosinophils, mast cells, monocytes,and others. In some embodiments, the compositions and methodsspecifically inhibit the interaction between SCF248 and c-Kit. Forexample, in some embodiments, the compositions and methods specificallyinhibit the interaction between SCF248 on myofibroblasts and c-Kit onimmune cells. As another example, in some embodiments, the compositionsand methods provided herein specifically inhibit the interaction betweenSCF248 on myofibrobalsts, activated epithelia, endothelia, macrophages,eosinophils, mast cells, and/or monocytes; with c-Kit on immune cellsand/or structural cells. In some embodiments, the methods comprisecontacting SCF248 on myofibroblasts with an antibody or fragment thereofprovided herein. In some embodiments, the antibody or fragment thereofprovided herein blocks binding of SCF248 to c-Kit. In some embodiments,the blocking is via steric hindrance. In some embodiments, the antibodyor fragment thereof provided herein internalizes SCF248.

In some embodiments, the present disclosure provides methods forinhibiting inflammation in a subject in need thereof, the methodcomprising administering to the subject an antibody or fragment thereofprovided herein. In some embodiments, the present disclosure providesmethods for inhibiting an inflammatory disease in a subject in needthereof, the method comprising administering to the subject an antibodyor fragment thereof provided herein. In further embodiments, theinflammatory disease is a chronic inflammatory disease. In someembodiments, the present disclosure provides methods for treatinginflammation and/or a chronic inflammatory disease in a subject in needthereof, the method comprising administering to the subject an antibodyor fragment thereof provided herein.

In some embodiments, the present disclosure provides methods forinhibiting fibrosis in a subject in need thereof, the method comprisingadministering to the subject an antibody or fragment thereof providedherein. In some embodiments, the present disclosure provides methods fortreating a fibrotic disease in a subject in need thereof, the methodcomprising administering to the subject an antibody or fragment thereofprovided herein. In embodiments, the method further comprisesadministering one or more additional therapy and/or therapeutic agent.

In some embodiments, the inflammatory disease or fibrotic disease isselected from the group consisting of urticaria, atopic dermatitis,bullous pemphigoid, scleroderma, systemic sclerosis, non-alcoholicsteatohepatitis (NASH), primary sclerosing cholangitis, liver cirrhosis,pulmonary fibrosis (e.g., idiopathic pulmonary fibrosis (IPF),scleroderma lung fibrosis), chronic obstructive pulmonary disease(COPD), acute respiratory distress syndrome (ARDS), cystic fibrosis,peribronchial fibrosis, hypersensitivity pneumonitis, asthma, bleomycinlung, endomyocardial fibrosis, fibromyalgia, eosinophilic esophagitis,radiation fibrosis, rheumatoid arthritis, and inflammatory boweldisease.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 provides a schematic overview of the tissue injury/inflammatorydisease process.

FIG. 2 shows an exemplary mechanism of an anti-SCF248 antibody of theinstant disclosure, 5H10. The 5H10 antibody is referred to in the figureas “OpSCF”.

FIG. 3 shows the isoforms of SCF, SCF220 and SCF 248; and the monomericcleaved extracellular domain, SCF165. SCF165 is released upon cleavageof SCF248 at its cleavage site within the Exon 6 region.

FIG. 4A is a set of histograms showing the binding of murine 5H10antibody to control cells that do not expression SCF (left panel), cellsthat express SCF220 but not SCF248 (middle panel), and cells thatexpress SCF248 but not SCF220 (right panel).

FIG. 4B shows the binding of murine 5H10 antibody to the 165 amino acidcleaved SCF extracellular domain (ECD) versus the complete 194 aminoacid SCF ECD.

FIG. 5 shows the mean fluorescence intensity (MFI) as measured by flowcytometry after contacting cultured human IPF myofibroblasts with pHrodored-labeled 2G8, 5H10, or control IgG antibodies.

FIG. 6 shows the activation of the P13K/AKT pathway and the MEK/ERKpathway of c-kit signaling after contacting eosinophils with anSCF248-expressing cells in the presence of 5H10 antibody or IgG control.5H10 antibody significantly reduced activation of both pathways.

FIG. 7A-FIG. 7B shows binding by flow cytometry of murine 2G8 and murine5H10 antibodies to early (FIG. 7A) and late (FIG. 7B) passage Sl/Sl4hSCF248 (ATCC® CRL2454™) cells.

FIG. 8A-FIG. 8B shows binding of murine 2G8 and murine 5H10 to Sl/Sl4hSCF220 (ATCC® CRL2453™) cells (FIG. 8A) and Sl/Sl4 hSCF248 cells (FIG.8B) at early passage and to hygromycin B treated cells.

FIG. 9A-FIG. 9B shows binding of 2G8 humanized variants at differentantibody concentrations by flow cytometry to Sl/Sl4 hSCF220 cells (FIG.9A) and Sl/Sl4 hSCF248 cells (FIG. 9B).

FIG. 10A-FIG. 10B shows binding of 5H10 humanized variants at differentantibody concentrations by flow cytometry to Sl/Sl4 hSCF248 cells (FIG.10A) and Sl/Sl4 hSCF220 cells (FIG. 10B).

FIGS. 11A-FIG. 11D shows binding of 2G8 humanized variants (FIG. 11A)and 5H10 humanized variants (FIG. 11B, FIG. 11C, FIG. 11D) at differentantibody concentrations by flow cytometry to Sl/Sl4 hSCF248 cells. InFIG. 11C, the indicated VH is paired with VK3. In FIG. 11D, the 5H10antibody shown is VH1/VK3.

FIGS. 12A-12D show the change in mRNA level of the CCL11 (FIG. 12A),Collagen 1A1 (FIG. 12B), fibronectin (FIG. 12C), or collagen 3 (FIG.12D) after preincubation of human IPF myofibroblasts (Mfb) with apositive control (irrelevant antibody) or the antibody indicated undereach bar in the figure. The murine parent antibody is indicated as“5H10” in the figure; humanized 5H10 antibodies VH1/VK3, VH2/VK3,VH3/VK3, VH4/VK3, and VH5/VK3 were also tested as shown. Antibodyconcentrations tested were 1 μg/mL or 10 μg/mL.

FIG. 13 shows the internalization of pHrodo red labeled murine 5H10antibody, VH0/VK0 chimeric antibody, and humanized variants VH1/VK3 andVH2/VK3. Arrows point to exemplary cells exhibiting internalizedantibody.

FIG. 14 shows the effect of 5H10 humanized variants on PBMC viability.

FIG. 15A-FIG. 1511 shows the CD4+ T cell responses induced by theindicated 5H10 humanized variants in an EpiScreen™ time course T cellproliferation assay. Exenatide and KLH, shown in FIGS. 15G and 15H,respectively, are positive controls.

FIG. 16 shows variance analysis (ANOVA) of an EpiScreen™ time course Tcell proliferation assay.

FIG. 17 shows lung histology of bleomycin control animals (left panel)and animals treated with bleomycin and 5H10 (20 mg/kg). In the FIG. 5

FIG. 18 shows decreases in lung hydroxyproline in animals treated withbleomycin and control IgG vs. animals treated with bleomycin and 5H10(20 mg/kg; referred to in the figure as anti-SCF248).

FIG. 19 shows the body weight as a % of the weight measured at day 0,over time in naîve mice, mice treated with bleomycin to induce lungfibrosis, and control Ig antibody (Bleo+cIg), and mice treated withbleomycin and murine 5H10 antibody (referred to in the figure asanti-SCF248). Antibody was administered at the indicated timepoints.

FIG. 20 shows decreases in mRNA for inflammatory cytokine and markers ofmyofibroblast activation (TGFβ, CCL2, Col1a1, Fibronectin (fn), smoothmuscle actin (acta2), and stem cell factor (kitlg)) in animals treatedwith bleomycin and control IgG vs. animals treated with bleomycin and5H10 (20 mg/kg; referred to in the figure as anti-SCF248).

FIG. 21 shows decreases in lung mast cells, eosinophils and ILC2lymphocytes in animals treated with bleomycin and control IgG vs.animals treated with bleomycin and 5H10 (20 mg/kg; referred to in thefigure as anti-SCF248).

FIG. 22 shows that pulmonary function testing as measured by forcedexpiratory volume (left panel), forced expiratory flow (middle panel),and change in pulmonary pressure (right panel) were significantlyimproved in animals treated with bleomycin and 5H10 (20 mg/kg; referredto in the figure as anti-SCF248) compared to animals treated withbleomycin and control IgG.

FIG. 23 shows a schematic of a study design in an in vivo chronicallergic asthma model used to test the humanized antibodies.

FIG. 24A-24E provide results of treatment with humanized 5H10 antibodiesin the in vivo model of chronic allergic asthma. FIG. 24A shows thatairway resistance as measured was significantly reduced in animalstreated with VH1/VK3 compared to PBS control. IL-13 mRNA (FIG. 24B),Collagen 1 mRNA (FIG. 24C), and Collagen 3 mRNA (FIG. 24D) in lungtissues were also reduced in animals treated with VH1/VK3 compared tothe chronic asthma (PBS) control. FIG. 24E shows that SCF248 mRNAexpression was also reduced in animals treated with VH1/VK3 5H10antibody compared to PBS control.

FIG. 25A-25C show that antibody VH1/VK3 reduced mRNA levels of mucusprotein Gob5 (FIG. 25A), IL-13 (FIG. 25B), and IL-5 (FIG. 25C), atconcentrations of 1 mg/kg and 5 mg/kg in vivo.

DETAILED DESCRIPTION

Stem Cell Factor (SCF) is a key mediator of acute and chronicinflammation, fibrotic diseases, and tissue remodeling diseases. Theinteraction of SCF with c-Kit on immune cells initiates and perpetuatesinflammation and fibrosis. The present disclosure provides compositionsand methods for inhibiting the interaction of SCF with c-Kit. In oneaspect, the present disclosure provides compositions and methods forpreventing the inflammatory form of SCF, SCF248, from interacting withc-Kit and thus reduces and/or prevents activation of immune cells. Thus,the present disclosure provides methods for treating chronicinflammation and fibrotic and tissue remodeling diseases. In one aspect,the present disclosure provides compositions and methods for reducingthe accumulation (e.g., proliferation and/or retention) of immune cellsin an organ or tissue. For example, the disclosure provides compositionsand methods that prevent SCF248 from interacting with c-Kit and thusreduces and/or prevents accumulation of immune cells in organs ortissues. In some embodiments, the disclosure provides compositions andmethods for reducing and/or preventing the activation and/oraccumulation in organs or tissues of mast cells, eosinophils, type 2innate lymphoid (ILC2) cells, and type 3 innate lymphoid (ILC3) cells.

In particular, the present disclosure provides antibodies and fragmentsthereof that specifically bind to SCF and block or inhibit itsinteraction with c-Kit. In some embodiments, the antibodies andfragments provided herein bind to SCF and inhibit the activity of c-Kitand c-Kit+ cells. The disclosure also provides methods for generatingantibodies and fragments thereof that specifically bind to SCF, as wellas diagnostic and therapeutic methods of use thereof. In one aspect, theantibodies and fragments thereof provided herein specifically bind tothe SCF isoform that drives inflammation, SCF248. Thus, the presentdisclosure provides specific, effective compositions and methods forinhibiting inflammation and fibrosis and treating chronic inflammatorydiseases and fibrotic diseases.

Definitions

As used herein, the term “antibody” refers to a binding protein havingat least one antigen binding domain. The antibodies and fragmentsthereof of the present invention may be whole antibodies or any fragmentthereof. Thus, the antibodies and fragments of the invention includemonoclonal antibodies or fragments thereof and antibody variants orfragments thereof, as well as immunoconjugates. Antigen bindingfragments include Fab fragments, Fab′ fragments, F(ab′)2 fragments,bispecific Fab dimers (Fab2), trispecific Fab trimers (Fab3), Fv, singlechain Fv proteins (“scFv”), bis-scFv, (scFv)2, minibodies, diabodies,triabodies, tetrabodies, disulfide stabilized Fv proteins (“dsFv”),single-domain antibodies (sdAb, nanobody), heavy-chain only antibodies(e.g., camelid VHH, camelid nanobody, shark Ig NAR), and portions offull length antibodies responsible for antigen binding. An isolatedantibody or antigen binding fragment thereof is one which has beenidentified and separated and/or recovered from a component of itsnatural environment.

In some embodiments, the antibodies and antigen binding fragmentsthereof are isolated antibodies and fragments thereof, Thus, the presentinvention provides isolated antibodies and antigen binding fragmentsthereof, and nucleic acids encoding such antibodies and fragments, aswell as compositions comprising such isolated antibodies, fragments, andnucleic acids. The term “isolated” refers to a compound of interest(e.g., an antibody or nucleic acid) that has been separated from itsnatural environment. The present invention further providespharmaceutical compositions comprising the isolated antibodies orfragments thereof, or nucleic acids encoding such antibodies orfragments, and further comprising one or more pharmaceuticallyacceptable carrier. Pharmaceutically acceptable carriers include, forexample, excipients, diluents, encapsulating materials, fillers,buffers, or other agents.

As used herein, the term “derived” when used to refer to a molecule orpolypeptide relative to a reference antibody or other binding protein,means a molecule or polypeptide that is specific for, and capable ofbinding to, the same epitope as the reference antibody or other bindingprotein.

As used herein, the phrase “specific for” may mean that the antibodydoes not bind to the target due to only non-specific interactions, andthis property can be determined by comparison to an isotype control orsimilar. Specific binding does not necessarily require, although it mayinclude, exclusive binding to a single target. In embodiments, theantibodies provided herein specifically bind to SCF248, and do not bindSCF220.

The term “host cell” means a cell that has been transformed, or iscapable of being transformed, with a nucleic acid sequence and therebyexpresses a gene of interest. The term includes the progeny of theparent cell, whether or not the progeny is identical in morphology or ingenetic make-up to the original parent cell, so long as the gene ofinterest is present.

A “variant” of a polypeptide (e.g., an antigen binding protein, or anantibody) comprises an amino acid sequence wherein one or more aminoacid residues are inserted into, deleted from and/or substituted intothe amino acid sequence relative to another polypeptide sequence.Variants include antibodies and fragments thereof that have a recitedpercent identity to an antibody or fragment provided herein or to anantibody or fragment having a recited DNA or amino acid sequence.

The term “identity” refers to a relationship between the sequences oftwo or more polypeptide molecules or two or more nucleic acid molecules,as determined by aligning and comparing the sequences. “Percentidentity,” “percent homology,” “sequence identity,” or “sequencehomology” and the like mean the percent of identical residues betweenthe amino acids or nucleotides in the compared molecules and iscalculated based on the size of the smallest of the molecules beingcompared. For these calculations, gaps in alignments (if any) arepreferably addressed by a particular mathematical model or computerprogram (i.e., an “algorithm”). Methods that can be used to calculatethe identity of the aligned nucleic acids or polypeptides include thosedescribed in Computational Molecular Biology, (Lesk, A. M., ed.), 1988,New York: Oxford University Press; Biocomputing Informatics and GenomeProjects, (Smith, D. W., ed.), 1993, New York: Academic Press; ComputerAnalysis of Sequence Data, Part I, (Griffin, A. M., and Griffin, H. G.,eds.), 1994, New Jersey: Humana Press; von Heinje, G., 1987, SequenceAnalysis in Molecular Biology, New York: Academic Press; SequenceAnalysis Primer, (Gribskov, M. and Devereux, J., eds.), 1991, New York:M. Stockton Press; and Carillo et al., 1988, SIAM J. Applied Math.48:1073. In calculating percent identity, the sequences being comparedare typically aligned in a way that gives the largest match between thesequences.

The term “light chain” includes a full-length light chain and fragmentsthereof having sufficient variable region sequence to confer bindingspecificity. A full-length light chain includes a variable region domainand a constant region domain. The variable region domain of the lightchain is at the amino-terminus of the polypeptide. Light chains includekappa chains and lambda chains.

The term “heavy chain” includes a full-length heavy chain and fragmentsthereof having sufficient variable region sequence to confer bindingspecificity. A full-length heavy chain includes a variable regiondomain, three constant region domains, C_(H)1, C_(H)2, and C_(H)3. Thevariable heavy domain is at the amino-terminus of the polypeptide, andthe C_(H) domains are at the carboxyl-terminus, with the C_(H)3 beingclosest to the carboxy-terminus of the polypeptide. Heavy chains can beof any isotype, including IgG (including IgG1, IgG2, IgG3 and IgG4subtypes), IgA (including IgA1 and IgA2 subtypes), IgM and IgE. The term“isotype” refers to the antibody class encoded by the heavy chainconstant region genes. In some embodiments, the antibodies providedherein have an IgG4 heavy chain, or an IgG4 heavy chain comprisingcertain amino acid mutations. For example, in some embodiments, the IgG4comprises a mutation at position 228 (EU numbering scheme, Kabat et al.Sequence of proteins of immunologic interest, 5th ed Bethesda, Md., NIH1991) to inhibit Fab arm exchange. For example, in some embodiments, theIgG4 heavy chain is an IgG4 S228P heavy chain. In some embodiments, theheavy chain comprises one or more amino acid mutations that reducebinding to Fc receptors, and thereby reduce or eliminate effectorfunction of the antibody. For example, the heavy chain may comprisemutations at one or more of positions 233, 234, 235, 236, 237, 265, 309,331, and 409 (EU numbering).

The term “variable region” or “variable domain” refers to a portion ofthe light and/or heavy chains of an antibody, typically includingapproximately the amino-terminal 120 to 130 amino acids in the heavychain and about 100 to 110 amino terminal amino acids in the lightchain. In certain embodiments, variable regions of different antibodiesdiffer extensively in amino acid sequence even among antibodies of thesame species. The variable region of an antibody typically determinesspecificity of a particular antibody for its target. The term “target,”as used herein, refers to a molecule or a portion of a molecule capableof being bound by an antigen binding protein. In certain embodiments, atarget can have one or more epitopes. In certain embodiments, a targetis an antigen. The use of “antigen” in the phrase “antigen bindingprotein” simply denotes that the protein sequence that comprises theantigen can be bound by an antibody. In this context, it does notrequire that the protein be foreign or that it be capable of inducing animmune response.

The term “epitope” includes any determinant capable being bound by anantigen binding protein, such as an antibody or to a T-cell receptor. Anepitope is a region of an antigen that is bound by an antigen bindingprotein that targets that antigen, and when the antigen is a protein,includes specific amino acids that directly contact the antigen bindingprotein. Most often, epitopes reside on proteins, but in some instancescan reside on other kinds of molecules, such as nucleic acids. Epitopedeterminants can include chemically active surface groupings ofmolecules such as amino acids, sugar side chains, phosphoryl or sulfonylgroups, and can have specific three dimensional structuralcharacteristics, and/or specific charge characteristics. Generally,antibodies specific for a particular target antigen will preferentiallyrecognize an epitope on the target antigen in a complex mixture ofproteins and/or macromolecules. Antibody epitopes may be linear orconformational. In embodiments, the epitope provided herein is a linearepitope.

The use of the singular includes the plural unless specifically statedotherwise. The word “a” or “an” means “at least one” unless specificallystated otherwise. The use of “or” means “and/or” unless statedotherwise. The meaning of the phrase “at least one” is equivalent to themeaning of the phrase “one or more.” Furthermore, the use of the term“including,” as well as other forms, such as “includes” and “included,”is not limiting. Also, terms such as “element” or “component” encompassboth elements or components comprising one unit and elements orcomponents comprising more than one unit unless specifically statedotherwise. As used herein, the term “about” refers to an amount more orless than the stated parameter value, for example plus or minus five orten percent of the object that “about” modifies, or as one of skill inthe art would recognize from the context (e.g., approximately 50% of theinterval between values). The term “about” also includes the valuereferenced.

Stem Cell Factor

In humans, there are at least two forms of SCF, which have differentstructures and activities. SCF220 functions in several homeostaticfunctions, including hematopoiesis and spermatogenesis and is found inbone marrow, testis, and other tissues and organs. SCF220 is slowlycleavable and sometimes called “membrane SCF.” In contrast, SCF248 israpidly cleavable and comprises a cleavage site in exon 6, locatedbetween the N-terminal c-kit binding domain and the transmembranedomain. SCF248 may be referred to as “soluble SCF”. Exon 6 is excludedfrom SCF220 via alternative splicing, and SCF220 thus lacks thiscleavage site. A monomeric, extracellular domain (SCF165) is thecleavage product and serves as a biomarker in plasma for chronicinflammatory diseases. Plasma may also contain detectable levels of SCFextracellular domain that comes from SCF220, but the majority ofdetectable extracellular domain is expected to be SCF165. SCF248 is theisoform found on myofibroblasts, activated epithelial cells, and othercells, which activates immune cells during inflammation and contributesto perpetuation of fibrosis. More specifically, SCF248 binds to c-Kit onimmune cells, initiating production of cytokines that activatefibroblasts to become myofibroblasts, which secrete extracellular matrixproteins, collagen, and fibronectin. The activated myofibroblasts aswell as activated epithelia, endothelia, macrophages, eosinophils, mastcells, monocytes, and other cells also express SCF on the cell surface,activating more c-Kit+ immune cells, resulting in further cytokinerelease and immune activation and fibrotic responses.

The antibodies and antigen-binding fragments thereof disclosed hereinare specific for SCF. In some embodiments, the antibodies and fragmentsthereof are specific for human SCF. In some embodiments, the antibodiesand fragments thereof are specific for SCF248. In some embodiments, theantibodies bind SCF248 and do not bind other isoforms of SCF. In someembodiments, the antibodies bind SCF248 and do not bind to SCF220. Insome embodiments, the present disclosure provides methods for making anantibody or fragment thereof that is specific for SCF248. Exemplaryantibodies and fragments that are specific for SCF248, as well asmethods for making and using the antibodies and fragments, are providedin the present disclosure. In some embodiments, the antibodies andfragments thereof provided herein breaks the positive feedback loopbetween SCF248 expressed on various cell types and cKit+ immune cells,by binding to SCF248 and blocking the interaction between SCF248 andc-Kit.

Antibodies and Fragments

The present disclosure provides antibodies, including monoclonalantibodies, and fragments thereof. The antibody fragments providedherein that are specific for SCF (e.g., SCF248) are sometimes referredto herein as antigen-binding fragments, meaning that they comprise theportion of the parent antibody that is capable of binding the targetantigen (SCF, e.g., SCF248). “Antibody fragment,” “antigen bindingfragment” and the like are used interchangeably herein. Examples ofantibody fragments include Fab fragments, Fab′ fragments, F(ab)′fragments, Fv fragments, isolated CDR regions, bispecific Fab dimers(Fab2), trispecific Fab trimers (Fab3), single chain Fv proteins(“scFv”), bis-scFv, (scFv)2, minibodies, diabodies, triabodies,tetrabodies, disulfide stabilized Fv proteins (“dsFv”), single-domainantibodies (sdAb, nanobody), heavy-chain only antibodies (e.g., camelidVHH, camelid nanobody, shark Ig NAR), and portions of full lengthantibodies responsible for antigen binding.

A “Fab fragment” comprises one light chain and the C_(H)1 and variableregions of one heavy chain. The heavy chain of a Fab molecule cannotform a disulfide bond with another heavy chain molecule. A “Fab′fragment” comprises one light chain and a portion of one heavy chainthat contains the VH domain and the C_(H)1 domain and also the regionbetween the C_(H)1 and C_(H)2 domains, such that an interchain disulfidebond can be formed between the two heavy chains of two Fab′ fragments toform an F(ab′)₂ molecule. A “F(ab′)2 fragment” contains two light chainsand two heavy chains containing a portion of the constant region betweenthe C_(H)1 and C_(H)2 domains, such that an interchain disulfide bond isformed between the two heavy chains. A F(ab′)₂ fragment thus is composedof two Fab′ fragments that are held together by a disulfide bond betweenthe two heavy chains. A “Fv fragment” comprises the variable regionsfrom both the heavy and light chains, but lacks the constant regions.“scFvs” are Fv molecules in which the heavy and light chain variableregions have been connected by a flexible linker to form a singlepolypeptide chain, which forms an antigen binding region.

In some aspects, the antibodies and fragments thereof provided hereinare defined by their complementary determining regions (CDRs). CDRs arepart of the variable chains in antibodies; each of the light and heavychain variable regions comprises three CDRs, CDR1, CDR2, and CDR3. TheCDRs of an antibody determine antigen specificity. In certainembodiments, definitive delineation of a CDR and identification ofresidues comprising the binding site of an antibody is accomplished bysolving the structure of the antibody and/or solving the structure ofthe antibody-ligand complex. In certain embodiments, that can beaccomplished by any of a variety of techniques known to those skilled inthe art, such as X-ray crystallography. In certain embodiments, variousmethods of analysis can be employed to identify or approximate the CDRregions. Examples of such methods include, but are not limited to, theKabat definition, the Chothia definition, the AbM definition and thecontact definition.

The Kabat definition is a standard for numbering the residues in anantibody and is typically used to identify CDR regions. See, e.g.,Johnson & Wu, Nucleic Acids Res., 28: 214-8 (2000). The Chothiadefinition is similar to the Kabat definition, but the Chothiadefinition takes into account positions of certain structural loopregions. See, e.g., Chothia et al., J. Mol. Biol., 196: 901-17 (1986);Chothia et al., Nature, 342: 877-83 (1989). The AbM definition uses anintegrated suite of computer programs produced by Oxford Molecular Groupthat model antibody structure. See, e.g., Martin et al., Proc Natl AcadSci (USA), 86:9268-9272 (1989); “AbM™, A Computer Program for ModelingVariable Regions of Antibodies,” Oxford, UK; Oxford Molecular, Ltd. TheAbM definition models the tertiary structure of an antibody from primarysequence using a combination of knowledge databases and ab initiomethods, such as those described by Samudrala et al., “Ab Initio ProteinStructure Prediction Using a Combined Hierarchical Approach,” inPROTEINS, Structure, Function and Genetics Suppl., 3:194-198 (1999). Thecontact definition is based on an analysis of the available complexcrystal structures. See, e.g., MacCallum et al., J. Mol. Biol., 5:732-45(1996).

Antibodies and fragments thereof may also include recombinantpolypeptides, fusion proteins, and bi-specific antibodies. The anti-SCFantibodies and fragments thereof disclosed herein may be of an IgG1,IgG2, IgG3, or IgG4 isotype. In one embodiment, the anti-SCF antibodiesand fragments thereof disclosed herein are of an IgG1 or an IgG4isotype. The anti-SCF antibodies and fragments thereof of the presentinvention may be derived from any species including, but not limited to,mouse, rat, rabbit, primate, llama, camel, goat, shark, chicken, andhuman. The SCF antibodies and fragments thereof may be chimeric,humanized, or fully human antibodies. In one embodiment, the anti-SCFantibodies are murine antibodies. In another embodiment, the anti-SCFantibodies are chimeric antibodies. In a further embodiment, thechimeric antibodies are mouse-human chimeric antibodies. In anotherembodiment, the antibodies are derived from mice and are humanized.

A “chimeric antibody” is an antibody having at least a portion of theheavy chain variable region and at least a portion of the light chainvariable region derived from one species; and at least a portion of aconstant region derived from another species. For example, in oneembodiment, a chimeric antibody may comprise murine variable regions anda human constant region.

A “humanized antibody” is an antibody containing complementaritydetermining regions (CDRs) that are derived from a non-human antibody;and framework regions as well as constant regions that are derived froma human antibody. For example, the anti-SCF antibodies provided hereinmay comprise CDRs derived from one or more murine antibodies and humanframework and constant regions. Thus, in one embodiment, the humanizedantibody provided herein binds to the same epitope on SCF as the murineantibody from which the antibody's CDRs are derived.

In some embodiments, the antibodies and fragments thereof providedherein comprise a heavy and light chain, each of which comprises threeCDRs. The amino acid sequences of exemplary heavy chain CDR1, CDR2, andCDR3 (HCDR1, HCDR2, and HCDR3, respectively) and light chain CDR1, CDR2,and CDR3 (LCDR1, LCDR2, and LCDR3, respectively) are provided below inTable 1. Table 1 also provides the amino acid sequences of exemplaryheavy and light chain variable regions. In some embodiments, the presentdisclosure provides antibodies referred to herein as “5H10” and “2G8”.The heavy chain variable regions of humanized 5H10 or 2G8 are referredto herein as VH1, VH2, VH3, VH4, and VH5. 5H10 VH0 is the variable heavychain of the murine parent antibody generated via the methods describedherein. VH1, VH2, VH3, VH4, and VH5 are each humanized heavy chainvariable regions derived from 5H10 VH0 or 2G8 VH0. The 5H10 antibodycomprises a kappa light chain. The murine parent antibody variable lightchain is referred to herein as 5H10 VK0. VK1, VK2, VK3, and VK4 are eachhumanized light chain variable regions derived from VK0. The 2G8antibody comprises a lambda light chain. The murine parent antibodyvariable light chain is referred to herein as 2G8 VL0. VL1, VL2, VL3,and VL4 are each humanized light chain variable regions derived fromVL0.

TABLE 1 Exemplary anti-SCF antibody sequences SEQ ID NO Description 15H10 Heavy SYWMN chain CDR1 2 5H10 Heavy QIYPGDGDTHYNGKFKG chain CDR2 35H10 Heavy SNWVGSY chain CDR3 4 5H10 Light KSSQSLLESDGKTYLN chain CDR1 55H10 Light LVSRLDS chain CDR2 6 5H10 Light WQGTHLPQT chain CDR3 75H10 Heavy QVQLQQSGAELVRPGSSVKISCKSSGYAFSSYWMNWVKQRPGQG chain variableLEWIGQIYPGDGDTHYNGKFKGKATLTADKSSSTAYMQLSRLTSE region VH0DSAVYFCSSSNWVGSYWGQGTLVTVSA (murine parent) 8 5H10 HeavyQVQLVQSGAELKKPGSSVKISCKSSGYAFSSYWMNWVKQRPGQG chain variableLEWIGQIYPGDGDTHYNGKFKGKATLTADKSTSTAYMELSSLTSE region VH1DSAVYFCSSSNWVGSYWGQGTLVTVSS (humanized) 9 5H10 HeavyQVQLVQSGAEVKKPGSSVKISCKSSGYAFSSYWMNWVKQRPGQG chain variableLEWIGQIYPGDGDTHYNGKFKGKATLTADKSTSTAYMELSSLRSE region VH2DTAVYFCSSSNWVGSYWGQGTLVTVSS (humanized) 10 5H10 HeavyQVQLVQSGAEVKKPGSSVKVSCKSSGYAFSSYWMNWVRQRPGQ chain variableGLEWIGQIYPGDGDTHYNGKFKGKATLTADKSTSTAYMELSSLRS region VH3EDTAVYFCSSSNWVGSYWGQGTLVTVSS (humanized) 11 5H10 HeavyQVQLVQSGAEVKKPGSSVKVSCKSSGYAFSSYWMNWVRQRPGQ chain variableGLEWIGQIYPGDGDTHYNGKFKGRVTITADKSTSTAYMELSSLRSE region VH4DTAVYFCSSSNWVGSYWGQGTLVTVSS (humanized) 12 5H10 HeavyQVQLVQSGAEVKKPGSSVKVSCKSSGYAFSSYWMNWVRQRPGQ chain variableGLEWIGQIYPGDGDTHYNGKFQGRVTITADKSTSTAYMELSSLRSE region VH5DTAVYYCSSSNWVGSYWGQGTLVTVSS (humanized) 13 5H10 LightDVVMTQTPLTLSVTIGQTASISCKSSQSLLESDGKTYLNWLSQRPG chain variableQSPKRLIYLVSRLDSGVPDRFTGSGSGTDFTLKISRVEAEDLGVYY region VK0CWQGTHLPQTFGGGTKLEIK (murine parent) 14 5H10 LightDVVMTQSPLTLSVTLGQPASISCKSSQSLLESDGKTYLNWLQQRPG chain variableQSPRRLIYLVSRLDSGVPDRFTGSGSGTDFTLKISRVEAEDVGVYY region VK1CWQGTHLPQTFGGGTKVEIK (humanized) 15 5H10 LightDVVMTQSPLSLPVTLGQPASISCKSSQSLLESDGKTYLNWLQQRPG chain variableQSPRRLIYLVSRLDSGVPDRFTGSGSGTDFTLKISRVEAEDVGVYY region VK2CWQGTHLPQTFGGGTKVEIK (humanized) 16 5H10 LightDVVMTQSPLSLPVTLGQPASISCKSSQSLLESDGKTYLNWLQQRPG chain variableQSPRRLIYLVSRLDSGVPDRFSGSGSGTDFTLKISRVEAEDVGVYY region VK3CWQGTHLPQTFGGGTKVEIK (humanized) 17 5H10 LightDVVMTQSPLSLPVTLGQPASISCKSSQSLLESDGKTYLNWFQQRPG chain variableQSPRRLIYLVSRLDSGVPDRFSGSGSGTDFTLKISRVEAEDVGVYY region VK4CWQGTHLPQTFGGGTKVEIK (humanized) 37 5H10 VH5 QIYPGDGDTHYNGKFQG CDR2

The skilled person will understand that the variable heavy and variablelight chains may be independently selected, or mixed and matched, fromthe antibodies provided herein. Thus, in some embodiments, theantibodies and fragments thereof provided herein comprise heavy andlight chain combinations selected from the group consisting of VH0/VK0,VH0/VK1, VH0/VK2, VH0/VK3, VH0/VK4, VH1/VK0, VH1/VK1, VH1/VK2, VH1/VK3,VH1/VK4, VH2/VK0, VH2/VK1, VH2/VK2, VH2/VK3, VH2/VK4, VH3/VK0, VH3/VK1,VH3/VK2, VH3/VK3, VH3/VK4, VH4/VK0, VH4/VK1, VH4/VK2, VH4/VK3, VH4/VK4,VH5/VK0, VH5/VK1, VH5/VK2, VH5/VK3, and VH5/VK4.

In some embodiments, the present disclosure provides antibodies orfragments comprising amino acid sequences having at least 80%, at least85%, at least 90%, at least 95%, or at least 99% homology to an aminoacid sequence selected from the group consisting of SEQ ID NOs: 7-12. Insome embodiments, the present disclosure provides antibodies orfragments thereof comprising a heavy chain variable region according toa sequence selected from the group consisting of SEQ ID NOs: 7-12. Insome embodiments, the present disclosure provides antibodies orfragments comprising amino acid sequences having at least 80%, at least85%, at least 90%, at least 95%, or at least 99% homology to an aminoacid sequence selected from the group consisting of SEQ ID NOs: 7-11,wherein the antibody or fragment comprises a heavy chain CDR1, CDR2, andCDR3 identical to SEQ ID NOs: 1, 2, and 3, respectively. In someembodiments, the present disclosure provides antibodies or fragmentscomprising amino acid sequences having at least 80%, at least 85%, atleast 90%, at least 95%, or at least 99% homology to an amino acidsequence of SEQ ID NO: 12, wherein the antibody or fragment comprises aheavy chain CDR1, CDR2, and CDR3 identical to SEQ ID NOs: 1, 37, and 3,respectively.

In some embodiments, the present disclosure provides antibodies orfragments comprising amino acid sequences having at least 80%, at least85%, at least 90%, at least 95%, or at least 99% homology to an aminoacid sequence selected from the group consisting of SEQ ID NOs: 13-17.In some embodiments, the present disclosure provides antibodies orfragments thereof comprising a light chain variable region according toa sequence selected from the group consisting of SEQ ID NOs: 13-17. Insome embodiments, the present disclosure provides antibodies orfragments comprising amino acid sequences having at least 80%, at least85%, at least 90%, at least 95%, or at least 99% homology to an aminoacid sequence selected from the group consisting of SEQ ID NOs: 13-17,wherein the antibody or fragment comprises a light chain CDR1, CDR2, andCDR3 identical to SEQ ID NOs: 4, 5, and 6, respectively.

In some embodiments, the present disclosure provides antibodies orfragments comprising amino acid sequences having at least 80%, at least85%, at least 90%, at least 95%, or at least 99% homology to: SEQ ID NO:7 and SEQ ID NO: 13; SEQ ID NO: 7 and SEQ ID NO: 14; SEQ ID NO: 7 andSEQ ID NO: 15; SEQ ID NO: 7 and SEQ ID NO: 16; SEQ ID NO: 7 and SEQ IDNO: 17; SEQ ID NO: 7 and SEQ ID NO: 13; SEQ ID NO: 7 and SEQ ID NO: 14;SEQ ID NO: 7 and SEQ ID NO: 15; SEQ ID NO: 7 and SEQ ID NO: 16; SEQ IDNO: 7 and SEQ ID NO: 17; SEQ ID NO: 8 and SEQ ID NO: 13; SEQ ID NO: 8and SEQ ID NO: 14; SEQ ID NO: 8 and SEQ ID NO: 15; SEQ ID NO: 8 and SEQID NO: 16; SEQ ID NO: 8 and SEQ ID NO: 17; SEQ ID NO: 9 and SEQ ID NO:13; SEQ ID NO: 9 and SEQ ID NO: 14; SEQ ID NO: 9 and SEQ ID NO: 15; SEQID NO: 9 and SEQ ID NO: 16; SEQ ID NO: 9 and SEQ ID NO: 17; SEQ ID NO:10 and SEQ ID NO: 13; SEQ ID NO: 10 and SEQ ID NO: 14; SEQ ID NO: 10 andSEQ ID NO: 15; SEQ ID NO: 10 and SEQ ID NO: 16; SEQ ID NO: 10 and SEQ IDNO: 17; SEQ ID NO: 11 and SEQ ID NO: 13; SEQ ID NO: 11 and SEQ ID NO:14; SEQ ID NO: 11 and SEQ ID NO: 15; SEQ ID NO: 11 and SEQ ID NO: 16;SEQ ID NO: 11 and SEQ ID NO: 17; SEQ ID NO: 12 and SEQ ID NO: 13; SEQ IDNO: 12 and SEQ ID NO: 14; SEQ ID NO: 12 and SEQ ID NO: 15; SEQ ID NO: 12and SEQ ID NO: 16; or SEQ ID NO: 12 and SEQ ID NO: 17.

In particular embodiments, the antibodies and fragments thereof compriseheavy and light chain combinations selected from the group consisting ofVH1/VK1, VH1/VK2, VH1/VK3, VH2/VK1, VH2/VK2, VH2/VK3, VH3/VK1, VH3/VK2,VH3/VK3, VH4/VK1, VH4/VK2, VH4/VK3, VH5/VK1, VH5/VK2, and VH5/VK3. Insome embodiments, the antibodies comprise an amino acid sequence havingat least 80%, at least 85%, at least 90%, at least 95%, or at least 99%sequence identity to SEQ ID NO: 8 or SEQ ID NO: 9; and an amino acidsequence having at least 80%, at least 85%, at least 90%, at least 95%,or at least 99% sequence identity to SEQ ID NO: 16. In some embodiments,the antibody, or fragment thereof, comprises an amino acid sequencehaving at least 80%, at least 85%, at least 90%, at least 95%, or atleast 99% sequence identity to SEQ ID NO: 8 or SEQ ID NO: 9; and anamino acid sequence having at least 80%, at least 85%, at least 90%, atleast 95%, or at least 99% sequence identity to SEQ ID NO: 16; whereinthe antibody or fragment comprises a heavy chain CDR1, CDR2, and CDR3identical to SEQ ID NOs: 1, 2, and 3, respectively, and a light chainCDR1, CDR2, and CDR3 identical to SEQ ID NOs: 4, 5, and 6, respectively.In some embodiments, the antibody, or fragment thereof, comprises anamino acid sequence having at least 95% or at least 99% sequenceidentity to SEQ ID NO: 8 or SEQ ID NO: 9; and an amino acid sequencehaving at least 95% or at least 99% sequence identity to SEQ ID NO: 16;wherein the antibody or fragment comprises a heavy chain CDR1, CDR2, andCDR3 identical to SEQ ID NOs: 1, 2, and 3, respectively, and a lightchain CDR1, CDR2, and CDR3 identical to SEQ ID NOs: 4, 5, and 6,respectively. The antibody or fragment thereof may specifically bind toSCF248 but may not bind to SCF220. In some embodiments, the antibodiescomprise a heavy chain variable region according to SEQ ID NO: 8 and alight chain variable region according to SEQ ID NO: 16. In someembodiments, the antibodies comprise a heavy chain variable regionaccording to SEQ ID NO: 9 and a light chain variable region according toSEQ ID NO: 16.

In some embodiments, the antibodies and fragments provided hereincomprise a heavy chain variable region amino acid sequence according toSEQ ID NO: 7, 8, 9, 10, 11, or 12, or a variant thereof; and/or comprisea light chain variable region amino acid sequence according to SEQ IDNO: 13, 14, 15, 16, or 17, or a variant thereof. Variants may comprise1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acid substitutions or deletions,or a combination thereof. In some embodiments, the amino acidsubstitutions are conservative substitutions. The anti-SCF antibodiesdisclosed herein having one or more amino acid substitution, insertion,deletion, or combination thereof in the CDR or variable light or heavychain region retain the biological activity of the correspondinganti-SCF antibody that does not have an amino acid substitution,insertion, or deletion relative to the sequences provided herein. Thus,the variant anti-SCF antibodies provided herein retain specific bindingto SCF248. The terms percent homology, sequence identity, sequencehomology, and the like are used interchangeably herein and refer to thenumber of identical amino acid sequences shared by two referencesequences, divided by the total number of amino acid positions,multiplied by 100.

In some embodiments, the present invention provides antibodies that bindto the same epitope as any one of the exemplary antibodies disclosedherein. Thus, in some embodiments, the present invention providesantibodies that compete for binding to SCF with the exemplary antibodiesprovided herein. For example, in some embodiments, the presentdisclosure provides antibodies that specifically bind to a region of theamino acid sequence provided herein as SEQ ID NO: 29. In someembodiments, antibodies provided herein specifically bind to an epitopecomprising the amino acid sequence of SEQ ID NO: 33 (ASSLRNDSSSSNRK) orSEQ ID NO: 36 ASSLRNDSSSSNR). In some embodiments, the presentdisclosure provides antibodies that specifically bind to an epitopeconsisting of an amino acid sequence according to SEQ ID NO: 33 or SEQID NO: 36. In some embodiments, the present disclosure providesantibodies that specifically bind to an epitope comprising at least 5,at least 6, at least 7, at least 8, at least 9, or at least 10contiguous amino acids of SEQ ID NO: 33.

In some embodiments, the antibodies and fragments thereof providedherein comprise the HCDR1, HCDR2, HCDR3, LCDR1, LCDR2, and/or LCDR3 ofthe heavy and light chain variable regions provided herein, or variantsthereof. Thus, in some embodiments, the antibodies and fragments thereofprovided herein include antibodies wherein the HCDRs are the HCDRs ofSEQ ID NO: 7, 8, 9, 10, 11, or 12; and/or wherein the LCDRs are theLCDRs of SEQ ID NOs: 13, 14, 15, 16, or 17. For example, in someembodiments, the antibodies and fragments thereof comprise amino acids31-35, 50-65, and 95-102 of any one of the heavy chain variable regionsprovided herein, as defined by the Kabat numbering scheme. In someembodiments, the antibodies and fragments thereof comprise amino acids24-34, 50-56, and 89-97 of any one of the light chain variable regionsprovided herein, as defined by the Kabat numbering scheme.

Exemplary humanized antibodies are provided herein. Additional anti-SCFantibodies comprising the heavy and light chain CDRs provided herein, orvariants thereof, may be generated using any human framework sequence,and are also encompassed in the present invention. In one embodiment,framework sequences suitable for use in the present invention includethose framework sequences that are structurally similar to the frameworksequences provided herein. Further modifications in the frameworkregions may be made to improve the properties of the antibodies providedherein. Such further framework modifications may include chemicalmodifications; point mutations to reduce immunogenicity or remove T cellepitopes; or back mutation to the residue in the original germlinesequence.

In some embodiments, such framework modifications include thosecorresponding to the mutations exemplified herein, includingbackmutations to the germline sequence. For example, in one embodiment,one or more amino acids in the human framework regions of the VH and/orVL of the humanized antibodies provided herein are back mutated to thecorresponding amino acid in the parent murine antibody. The presentinvention also encompasses humanized antibodies that bind to SCF (e.g.,SCF248) and comprise framework modifications corresponding to theexemplary modifications described herein with respect to any suitableframework sequence, as well as other framework modifications thatotherwise improve the properties of the antibodies. In otherembodiments, the antibodies provided herein comprise one or moremutations to improve stability, improve solubility, alter glycosylation,and/or reduce immunogenicity, such as, for example, by targeted aminoacid changes that reduce deamidation or oxidation, reduce isomerization,optimize the hydrophobic core and/or charge cluster residues, removehydrophobic surface residues, optimize residues involved in theinterface between the variable heavy and variable light chains, and/ormodify the isoelectric point.

The anti-SCF antibodies and fragments thereof provided herein mayfurther comprise Fc region modifications to alter effector functions. Fcmodifications may be amino acid insertions, deletions, or substitutions,or may be chemical modifications. For example, Fc region modificationsmay be made to increase or decrease complement binding, to increase ordecrease antibody-dependent cellular cytoxicity, or to increase ordecrease the half-life of the antibody. Some Fc modifications increaseor decrease the affinity of the antibody for an Fcγ receptor such asFcγRI, FcγRII, FcγRIII, or FcRn. Various Fc modifications have beendescribed in the art, for example, in Shields et al., J Biol. Chem 276;6591 (2001); Tai et al. Blood 119; 2074 (2012); Spiekermann et al. JExp. Med 196; 303 (2002); Moore et al. mAbs 2:2; 181 (2010);Medzihradsky Methods in Molecular Biology 446; 293 (2008); Mannan et al.Drug Metabolism and Disposition 35; 86 (2007); and Idusogie et al. JImmunol 164; 4178 (2000). In some embodiments, Fc region glycosylationpatters are altered. In other embodiments, the Fc region is modified bypegylation (e.g., by reacting the antibody or fragment thereof withpolyethylene glycol (PEG). Exemplary Fc modifications includemodifications at one or more amino acid position selected from the groupconsisting of 228, 233, 234, 235, 236, 241, 248, 265, 297, 309, 331, and409 (Kabat numbering; Kabat et al., Sequences of Immunological Interest,Fifth Edition, National Institute of Health, Bethesda, Md. (1991)). Inembodiments, the antibody has modifications to reduce or abolisheffector function. In embodiments, the antibody is an IgG1 antibodyhaving one or more Fc modification selected from the group consisting ofE233P, L234V, L234A, L235V, L235A, G236 (deleted), D265A, D270A, N297Aand N297Q. In embodiments, the antibody is an IgG4 antibody having oneor more Fc modification selected from the group consisting of S228P,E233P, F234A, F234V, L235A, L235V, S241P, L248E, D265A, D265T, L309L,and R409K. In embodiments, the anti-SCF antibodies provided hereincomprise a S241P mutation and an L248E mutation.

In embodiments, the present disclosure provides antibodies providedherein that comprise a human IgG4 constant region according to SEQ IDNOs: 40 and 41. In embodiments, the present disclosure providesantibodies comprising at least about 80%, at least about 85%, at leastabout 90%, at least about 95%, or about 99% sequence identity to SEQ IDNO: 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, or 50. In embodiments, thepresent disclosure provides antibodies comprising a heavy chainaccording to SEQ ID NO: 40 and a light chain according to SEQ ID NO: 41.In embodiments, the present disclosure provides antibodies comprising aheavy chain according to SEQ ID NO: 42, 43, 44, 45, or 46 and a lightchain according to SEQ ID NO: 47, 48, 49, or 50. In embodiments, thepresent disclosure provides an antibody comprising a heavy chainaccording to SEQ ID NO: 42 and a light chain according to SEQ ID NO: 49.In embodiments, the present disclosure provides an antibody comprising aheavy chain according to SEQ ID NO: 43 and a light chain according toSEQ ID NO: 49. In embodiments, the present disclosure provides anantibody comprising a heavy chain according to SEQ ID NO: 44 and a lightchain according to SEQ ID NO: 49. In embodiments, the present disclosureprovides an antibody comprising a heavy chain according to SEQ ID NO: 45and a light chain according to SEQ ID NO: 49. In embodiments, thepresent disclosure provides an antibody comprising a heavy chainaccording to SEQ ID NO: 46 and a light chain according to SEQ ID NO: 49.

In some embodiments, the present disclosure provides methods for makingantibodies that specifically bind to SCF248. The SCF248 isoform of SCFinclude exon 6, which comprises a cleavage site between two alanineresidues (amino acids 16 and 17 of SEQ ID NO: 34, which provides theamino acid sequence of exon 6). Previous anti-SCF antibodies weregenerated by immunizing mice with a peptide spanning exon 6 and part ofExon 7 (see, e.g., U.S. Pat. No. 8,911,729, which is hereby incorporatedby reference in its entirety for all purposes). Since SCF220 isassociated with homeostatic activities, any cross-reactivity with SCF220would be detrimental as it would result in various off-target effects insubjects. Advantageously, the antibodies provided in the presentdisclosure bind to SCF248 with very high specificity. In someembodiments, the antibodies provided herein are specific for SCF248 anddo not bind to SCF220. Thus, the antibodies provided herein are capableof specifically inhibiting the interaction between SCF248 and c-Kit thatinduces and perpetuates chronic inflammatory responses and fibrosis.Moreover, the antibodies provided herein are capable of specificallyinducing the internalization of SCF and thereby reducing the interactionbetween SCF248 and c-Kit. Accordingly, in some embodiments the presentdisclosure provides antibodies that are specific for SCF248 and are safeand effective in various inflammatory and fibrotic diseases discussedherein and known in the art.

For preparation of monoclonal antibodies, any technique that providesfor the production of antibody molecules by continuous cell lines inculture may be used (see e.g., Harlow and Lane, Antibodies: A LaboratoryManual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.).These include, but are not limited to, the hybridoma techniqueoriginally developed by Köhler and Milstein and the trioma technique,the human B-cell hybridoma technique (See, e.g., Kozbor et al., Immunol.Today, 4:72 (1983)), and the EBV-hybridoma technique to produce humanmonoclonal antibodies (Cole et al., in Monoclonal Antibodies and CancerTherapy, Alan R. Liss, Inc., pp. 77-96 (1985)). Alternatively, theantibodies may be made by recombinant DNA methods. In some embodiments,antibodies in accordance with the present disclosure may be made byisolating monoclonal antibodies from phage display libraries using thetechniques described, for example, in Clackson et al., Nature 352:624-28(1991) and Marks et al., J. Mol. Biol. 222(3):581-97 (1991). In someembodiments, the antibodies are fully human antibodies constructed bycombining Fv clone variable domain sequence(s) selected fromhuman-derived phage display or yeast display libraries with known humanconstant domain sequence(s).

In some embodiments provided herein, the antibodies are prepared from ahybridoma. Using the hybridoma method, a mouse, hamster, or otherappropriate host animal, is immunized by injecting an immunizing peptideto elicit the production by lymphocytes of antibodies that willspecifically bind to an immunizing antigen. Alternatively, lymphocytescan be immunized in vitro. Following immunization, the lymphocytes areisolated and fused with a suitable myeloma cell line using, for example,polyethylene glycol, to form hybridoma cells that can then be selectedaway from unfused lymphocytes and myeloma cells. Hybridomas that producemonoclonal antibodies directed specifically against a chosen antigen asdetermined by immunoprecipitation, immunoblotting, or by an in vitrobinding assay such as radioimmunoassay (MA) or enzyme-linkedimmunosorbent assay (ELISA) can then be propagated in vitro (e.g., inculture) using standard methods (Goding, Monoclonal Antibodies:Principles and Practice, Academic Press, 1986) or in vivo as ascitestumors in an animal. The monoclonal antibodies can then be purified fromthe culture medium or ascites fluid as described for polyclonalantibodies above.

In some embodiments, the antibodies provided herein are generated usingthe murine hybridoma system. Hybridoma production in the mouse is awell-established procedure. Immunization protocols and techniques forisolation of immunized splenocytes for fusion are known in the art.Fusion partners (e.g., murine myeloma cells) and fusion procedures arealso known. Embodiments of the technology herein provide antibodies(e.g., monoclonal antibodies) produced from a hybridoma prepared byimmunizing mice with a peptide that is a portion or fragment of the SCFprotein.

In some embodiments, the antibodies specific for SCF248 provided hereinare generated by immunizing mice with a peptide having an amino acidsequence that is largely or exclusively within exon 6. For example, theimmunizing peptide comprises any stretch of 5 or more amino acids withinSEQ ID NO: 34. As another example, the immunizing peptide comprises anystretch of 5 or more amino acids beginning at amino acid position 20 ofSEQ ID NO: 29. As another example, the immunizing peptide comprises astretch of 5 or more amino acids beginning at amino acid position 20 ofSEQ ID NO: 29 and ending at any one of positions 25 to 38 of SEQ ID NO:29. Thus, in some embodiments, the immunizing peptide comprises theamino acid sequence of exon 6 after the cleavage site, and is eitherfully contained within exon 6 or comprises only 1, 2, 3, 4, or 5 aminoacids of exon 7. In some embodiments, the immunizing peptide comprisesor consists of SEQ ID NO: 30. In some embodiments, the immunizingpeptide comprises any of the peptides provided herein or conservativevariants thereof. Conservative variants may comprise 1, 2, 3, 4, or 5amino acid substitutions or deletions, or a combination thereof. Asprovided above, in some embodiments, the antibodies generated using theimmunizing peptides provided herein have an epitope that falls entirelyor largely within exon 6. By “largely within” it is meant that at least75%, at least 80%, at least 85%, at least 90%, or at least 95% of thepeptide falls within exon 6. In some embodiments, the epitope begins atthe cleavage site of exon 6 (i.e., between the alanines at amino acidpositions 19 and 20 of SEQ ID NO: 29 and extends to the end of exon 6.In some embodiments, the epitope begins at the cleavage site of exon 6and extends to the 1^(st), 2^(nd), 3^(rd), 4^(th), or 5^(th) n-terminalamino acid of the transmembrane domain. In some embodiments, the epitopecomprises or consists of SEQ ID NO: 33. In some embodiments, theantibody referred to herein as 5H10 (including the murine, chimeric, andhumanized 5H10 antibodies) binds to an epitope of SCF comprising orconsisting of SEQ ID NO: 33.

In some embodiments, the methods provided herein were used to generateantibodies referred to herein as 5H10. In some embodiments, the antibody“5H10” is also referred to herein as “OpSCF.” Antibody 5H10advantageously binds SCF248 with high specificity and does not bindSCF220. The amino acid sequences of the murine parent antibody 5H10, aswell as humanized variants thereof, are provided herein (see, Table 1).

In one embodiment, the present invention provides bispecific ormultispecific antibodies specific for SCF and at least one other antigenor epitope. The anti-SCF antibodies and fragments thereof providedherein may be tested for binding to SCF using the binding assaysprovided herein, or any other binding assay known in the art.

Unless otherwise stated, the practice of the present invention employsconventional molecular biology, cell biology, biochemistry, andimmunology techniques that are well known in the art and described, forexample, in Methods in Molecular Biology, Humana Press; MolecularCloning: A Laboratory Manual, second edition (Sambrook et al., 1989),Current Protocols in Immunology (J. E. Coliganet al., eds., 1991);Immunobiology (C. A. Janeway and P. Travers, 1997); Antibodies (P.Finch, 1997); Antibodies: a practical approach (D. Catty., ed., IRLPress, 1988-1989); Monoclonal antibodies: a practical approach (P.Shepherd and C. Dean, eds., Oxford University Press, 2000); Phagedisplay: a laboratory manual (C. Barbas III et al, Cold Spring HarborLaboratory Press, 2001); and Using antibodies: a laboratory manual (E.Harlow and D. Lane (Cold Spring Harbor Laboratory Press, 1999).

Methods of Treatment

In one aspect, the present disclosure provides methods for treatingand/or preventing any disease or condition associated with immune cellmigration, activation, and/or proliferation via interaction of SCF248with c-Kit on immune cells. Thus, in some embodiments, the presentdisclosure provides methods for inhibiting or preventing activation ofimmune cells; as well as reducing or preventing the accumulation ofimmune cells within organs or tissues, thereby treating or preventingvarious diseases and disorders that involve inflammation. In someembodiments, the immune cells are selected from the group consisting ofmast cells, innate lymphoid cells (ILCs, such as ILC2 or ILC3 cells),and eosinophils.

As used herein, the terms “treatment” or “treating” refers to boththerapeutic treatment and prophylactic or preventive measures. Subjectsin need of treatment include those subjects that already have thedisease or condition, as well as those that may develop the disease orcondition and in whom the object is to prevent, delay, or diminish thedisease or condition. As used herein, the term “subject” denotes amammal, such as a rodent, a feline, a canine, and a primate. Preferably,a subject according to the invention is a human. The term“therapeutically effective amount,” as used herein, refers to the amountof a compound or composition that is necessary to provide a therapeuticand/or preventative benefit to the subject.

In one aspect the present invention provides methods for treating asubject for an inflammatory disease, a fibrotic disease, and/or a tissueremodeling disease. In some embodiments, the inflammatory disease is achronic inflammatory disease.

Chronic inflammatory, fibrotic, and tissue remodeling diseases includediseases of the lung, kidney, liver, heart, skin, connective tissue, andother tissues. Exemplary inflammatory, fibrotic or tissue remodelingdiseases include, without limitation, pulmonary fibrosis (e.g.,idiopathic pulmonary fibrosis (IPF), scleroderma lung fibrosis,scleroderma-related interstitial lung disease (SSc-ILD), pulmonaryfibrosis associated with a lung infection or pneumonia, pulmonaryfibrosis associated with systemic lupus erythematosus and/or rheumatoidarthritis, sarcoidosis), chronic obstructive pulmonary disease (COPD),acute respiratory distress syndrome (ARDS), cystic fibrosis,peribronchial fibrosis, bleomycin lung, hypersensitivity pneumonitis,asthma, fibrothorax, mediastinal fibrosis, chronic rhinosinusitis,urticaria (e.g., chronic spontaneous urticaria), atopic dermatitis,dermatomyositis, nodular subepidermal fibrosis, scleroderma, keloid,renal fibrosis, chronic kidney disease, glomerulonephritis, chronicrenal allograft rejection, nephropathy (e.g., IgA nephropathy, focalsegmental glomerulosclerosis, rapidly progressive glomerulonephritis,crescentic glomerulonephritis, lupus nephritis, hypertensivenephropathy, or diabetic nephropathy), non-alcoholic steatohepatitis(NASH), liver cirrhosis, hepatic fibrosis, primary sclerosingcholangitis, primary biliary cirrhosis, fibromyalgia, gingival fibrosis,radiation-induced fibrosis, eosinophilic esophagitis, arthrofibrosis,and atrial fibrosis, endomyocardial fibrosis, parenchymal fibrosis,fibrous histocytoma, or glial scarring.

In some embodiments, the antibodies and fragments thereof disclosedherein may be administered to the subject by at least one route selectedfrom parenteral, subcutaneous, intramuscular, intravenous,intrarticular, intrabronchial, intraabdominal, intracapsular,intracartilaginous, intracavitary, intracelial, intracerebellar,intracerebroventricular, intracolic, intracervical, intragastric,intrahepatic, intramyocardial, intraosteal, intrapelvic,intrapericardiac, intraperitoneal, intrapleural, intraprostatic,intrapulmonary, intrarectal, intrarenal, intraretinal, intraspinal,intrasynovial, intrathoracic, intratympanic, intrauterine, intravesical,intravitreal, bolus, subconjunctival, oral, vaginal, rectal, buccal,sublingual, intranasal, intratumoral, and transdermal.

In embodiments, the antibodies and fragments thereof disclosed hereinmay be administered to a subject in need thereof in combination with oneor more additional therapy. The one or more additional therapy may be aprocedure such as a surgical procedure, or may be a therapeutic agent,such as an agent designed to mitigate or reduce symptoms of a disease ordisorder associated with fibrosis and/or inflammation.

The present invention is further illustrated by reference to thefollowing Examples. However, it should be noted that these Examples,like the embodiments described above, are illustrative and are not to beconstrued as restricting the scope of the invention in any way.

EXAMPLES

The following examples are given for the purpose of illustrating variousembodiments of the disclosure and are not meant to limit the presentdisclosure in any fashion. Changes therein and other uses which areencompassed within the spirit of the disclosure, as defined by the scopeof the claims, will be recognized by those skilled in the art.

An overview of the tissue injury/disease process is summarized in FIG. 1. A disease process initiates inflammation. c-Kit+ immune cells producecytokines that cause fibroblasts to change into activated myofibroblastswhich express SCF248 on their surface. The expression of SCF248 on thesurface of myofibroblasts and other cells activates more immune cells,resulting in cytokine release of IL-4, IL-9, IL-13, IL-25, TGFβ, andother cytokines, perpetuating inflammation. Myofibroblasts secreteextracellular matrix proteins, collagen, and fibronectin, leading tofibrosis and remodeling diseases such as pulmonary fibrosis, skinfibrosis, severe asthma, and other diseases.

An exemplary mechanism of an antibody of the instant disclosure whichtargets SCF248 (said antibody referred to herein as OpSCF and/or as5H10) is summarized in FIG. 2 .

As provided above, SCF has two isoforms which result from alternativesplicing: SCF248 and SCF220. SCF248 and SCF220 differ by exon 6. SCF220is associated with homeostatic functions, and SCF248 is associated withinflammation and fibrosis. SCF248 activates immune cells duringinflammation and is sometimes called “soluble SCF.” SCF248 is expressedon various cell types including myofibroblasts, activated epithelia,endothelia, macrophages, eosinophils, mast cells, and monocytes (FIG. 3). The SCF248 isoform results in cleavage of monomeric cleavedextracellular domain, called SCF165. The amino acid sequence of exon 6is provided herein as SEQ ID NO: 34.

Example 1: Production of Anti-SCF mAbs Utilizing Hybridoma Technology

A peptide comprising ASSLRNDSSSSNRKAKNPPGD (SEQ ID NO: 30) was used togenerate antibodies that bind to SCF248. The immunization peptidecomprised a portion of exon 6, i.e. the SCF248 isoform of stem cellfactor. In particular, the immunization peptide comprised a portion ofexon 6 that begins after a cleavage site as defined herein. Mice wereimmunized with a peptide according to SEQ ID NO: 30 with a standardprotocol. The determination of high titer serum antibodies indicated theappropriate immunization and fusion hybridomas were made. Culturesupernatants were analyzed from individual clones for SCF-specificantibodies and chosen based upon specificity. Hybridomas producingspecific monoclonal antibodies against the peptide were propagated andthe monoclonal with the highest titer was subsequently tested inbiologically relevant cultures. Antibody 5H10 had high specificity forSCF248 and no cross-reactivity with SCF220. No other monoclonalantibodies produced by the hybridomas had high specificity for SCF248without cross-reactivity with SCF220. Thus, 5H10 was selected forfurther characterization, development, and chimerization and subsequenthumanization.

Example 2. 5H10 Binding to SCF248 Complete Extracellular Domain

The murine 5H10 antibody obtained as described in Example 1 was directlyconjugated with a fluorescent marker and the labeled antibody wasincubated with Sl/Sl4 hSCF248 cells, which express SCF248; Sl/Sl4hSCF220 cells, which express SCF220; or control cells that do notexpress SCF. Binding of the labeled antibody to the cells was assessedby flow cytometry. The specificity of 5H10 for SCF248 and lack ofcrossreactivity with SCF220 is shown in FIG. 4A.

Binding of the murine 5H10 antibody to the cleaved extracellular domain(ECD) containing only amino acids 1-165 of SCF, vs the complete ECDcontaining amino acids 1-194 of SCF, was assessed by an ELISA method.The antibody bound to the complete SCF ECD but not to the cleaved SCFECD (FIG. 4B), demonstrating that the antibody is specific for thecomplete extracellular domain and does not bind to the monomeric cleavedECD that circulates in blood.

To assess the ability of 2G8 and 5H10 antibodies to internalize SCF248on myofibroblasts, antibodies were labeled with pHrodo red, which iscolorless at neutral pH and fluoresces red at the low pH within anendosome. Labeled antibodies were incubated with cultured human IPFmyofibroblasts for 45 minutes and red fluorescence was visualized bymicroscopy. As shown in FIG. 5 , the dye-labeled antibodies, but notcontrol IgG, were rapidly internalized. 5H10 was internalized morerapidly and resulted in higher fluorescence compared to 2G8.

SCF triggers c-kit to signal by two distinct pathways: the MEK/ERKpathway and the P13K/AKT pathway. A study was conducted to determinewhether the murine 5H10 antibody inhibits intracellular signaling inc-kit positive cells in either or both of these pathways. Eosinophilswere incubated with SCF248-expressing cell lines, in the presence ofeither 5H10 or IgG control, and phospho-protein expression was measuredwith a BioRad Bio-Plex assay system. 5H10 significantly decreased thephospho-MEK and phosphor-AKT levels, indicating that the antibodysignificantly reduced c-kit mediated intracellular signaling (FIG. 6 ).

Taken together, the results of these studies indicated that antibody5H10 binds specifically to and internalizes SCF248, and does notcross-react with the SCF220 isoform or the cleaved ECD. Moreover, 5H10significantly inhibits the intracellular signaling pathways in c-kitpositive cells that perpetuate inflammation.

Example 3. Humanization of Murine Antibody 5H10

Chimeric antibodies derived from 5H10 were produced by subcloning thevariable domains of the heavy and light chains into a vector with ahuman IgG4 backbone. Chimeric antibodies were expressed and purifiedusing standard protocols. 2G8 is a previously developed antibody thatbinds to SCF248 and SCF220, and contains a lambda light chain. Thechimeric heavy and light chains of 2G8 were named VH0 and VL0,respectively. 5H10, the SCF248-specific antibody provided herein,contains a kappa light chain. The chimeric heavy and light chains of5H10 were named VH0 and VK0, respectively.

The chimeric antibodies were humanized. Humanized heavy chains retainedthe same complementarity-determining regions (CDRs) but more“human-like” framework regions, and several humanized variants of eachof 2G8 and 5H10 variable heavy chains, referred to herein as VH1, VH2,VH3, VH4, and VH5, were generated. Humanized kappa light chain variantsof 5H10, referred to herein as VK1, VK2, VK3, and VK4, were alsogenerated. Humanized lambda light chains of 2G8 were named VL1, VL2,VL3, and VL4. The 2G8 and 5H10 combinations of chimeric and humanizedlight chains and heavy chains tested are shown in Table 2 and Table 3,respectively. As shown in Table 2, certain heavy and light chaincombinations of the 5H10 antibody variants resulted in high binding tohSCF248. Binding data used to determine the binding score are providedbelow in Example 5.

TABLE 2 Binding score for 2G8 chimeric and humanized clones to Sl/Sl4hSCF248 cells 2G8 mAb Binding Score VH0/VL0 high VH1/VL1 Moderate highVH1/VL3 moderate VH1/VL4 Moderate VH2/VL1 Moderate VH2/VL4 ModerateVH3/VL1 Moderate VH3/VL4 Moderate VH4/VL1 Moderate VH4/VL2 ModerateVH5/VL1 Moderate high VH5/VL4 Moderate

TABLE 3 Binding score for 5H10 chimeric and humanized clones to Sl/Sl4hSCF248 cells 5H10 mAb Binding Score VH0/VK0 high VH1/VK1 High VH1/VK2High VH1/VK3 High VH1/VK4 No binding VH2/VK2 Moderate high VH2/VK3 highVH3/VK2 Moderate VH3/VK3 Moderate VH4/VK2 Moderate low VH4/VK3 Moderatelow VH5/VK2 Low VH5/VK3 low

Binding affinity was also assessed using a BiaCore analysis. BiaCoredata showed that the affinity for immobilized SCF248 peptide antigen ofall humanized 5H10 antibodies having the VK1, VK2, or VK3 light chainwas very similar to the binding affinity of the parental murine 5H10using this assay. Humanized 5H10 antibodies having a VK4 light chain didnot bind to the peptide.

TABLE 4 Biacore data VK0 VK1 VK2 VK3 VK4 VH0 1.00 0.91 VH1 0.92 0.990.97 0.94 — VH2 0.98 0.99 0.94 — VH3 1.15 1.16 1.10 — VH3 1.27 1.32 0.85— VH5 1.07 0.93 1.09 —

Example 4. Evaluation of Anti-SCF Chimeric Antibody Binding by FlowCytometry

Sl/Sl4 hSCF248 cells, a transfected cell line that express SCF248, wereutilized to test the binding of the chimeric antibodies 2G8 and 5H10. Ananti-SCF antibody was used as a positive control for SCF binding. Ahuman IgG4 antibody was used as a negative isotype control antibody.Sl/Sl4 hSCF248 cells at early passage (P3) were compared to cells atlater passage (P5). As expected, the negative control (human IgG4antibody) did not bind to either cell population. 5H10 bound to cells atearly passage (FIG. 7A), but was not detected at later passage (FIG.7B), due to loss of expression of SCF248 over multiple passages.Similarly, the maximum mean fluorescence intensity (MFI) detected with10 μg/mL of 2G8 was reduced approximately four times at P5 compared toP3.

Similar observations were seen with hygromycin B-treated cells.Hygromycin selection was used to enrich the fraction of Sl/Sl4 cellsexpressing the relevant human SCF sequence. The binding of the twochimeric anti-SCF mAbs 2G8 and 5H10 and humanized anti-SCF antibodieswere evaluated via flow cytometry. Sl/Sl4 hSCF248 cells and Sl/Sl4hSCF220 cells, which are SCF248+ and SCF220+, respectively were utilizedto test the binding and specificity of the chimeric antibodies 2G8 and5H10. An anti-SCF antibody was used as a positive control for SCFbinding. A human IgG4 antibody was used as a negative isotype controlantibody. Hygromycin B treated cells were compared to early passage (P3)cells. The maximum mean fluorescent intensities (MFIs) and antibody doseresponse curves were similar to early passage (P3) cells (FIG. 8A, FIG.8B).

Example 5. Binding Assessment of 2G8 and 5H10 Humanized mAbs by FlowCytometry

Sl/Sl4 hSCF248 cells and Sl/Sl4 hSCF220 cells, which are SCF248+ andSCF220+, respectively were utilized to test the binding and specificityof the chimeric antibodies 2G8 and 5H10, and humanized variants thereof.In both sets of experiments, a human IgG4 antibody was used as anegative isotype control antibody. The isotype control did not bind toSl/Sl4 hSCF248 cells or Sl/Sl4 hSCF220 cells (FIGS. 9A, 9B, 10A, and10B). The commercially available anti-SCF antibody (Abcam, Cat #EP665Y/ab52603) was found to bind Sl/Sl4 hSCF220 cells and weakly toSl/Sl4 hSCF248 cells (only at a 1:25 dilution) (FIGS. 9A, 9B, 10A, and10B). 2G8 VH0/VL0 (chimeric 2G8) exhibited stronger binding than itshumanized clones. However, 2G8 VH0/VL0 also showed binding to Sl/Sl4hSCF220 cells at antibody concentrations of 3.3 and 10 μg/mL (FIG. 9A,FIG. 9B). 5H10 VH0/VK0 showed higher binding compared to humanizedclones 5H10 VH3/VK2, 5H10 VH3/VK3, 5H10 VH4/VK2, 5H10 VH4/VK3, 5H10VH5/VK2, and 5H10 VH5/VK3 (FIG. 10A). No binding of 5H10 or anyhumanized variants thereof to Sl/Sl4 hSCF220 cells was observed (FIG.10B). Differences among the indicated 5H10 humanized variants in termsof 50% maximal binding (BC₅₀) in this study are shown in Table 5. Thebinding of the 5H10 clones reached saturation at 3.3 μg/mL on Sl/Sl4hSCF248 cells. (FIG. 10A).

TABLE 5 BC₅₀ (μg/mL) values for binding of chimeric and humanized 5H10variants, isotype control, and commercially available anti-SCF antibodyto Sl/Sl4 hSCF248 cells Sample ID BC₅₀ (μg/mL) 5H10 VH0/VK0 5.47 5H10VH3/VK2 1.36 5H10 VH3/VK3 0.90 5H10 VH4/VK2 1.91 5H10 VH4/VK3 1.18 5H10VH5/VK2 2.12 5H10 VH5/VK3 0.67 Isotype control n/a Anti-SCF Abeam 3.02

Sl/Sl4 hSCF248 cells were utilized to test the binding of additionalhumanized variants of 5H10 and 2G8. 2G8 VH0/VL0 (chimeric) showedstronger cell binding than the humanized variants (FIG. 11A). Thebinding profiles of the humanized 5H10 clones 5H10 VH1/VK1, 5H10VH1/VK2, 5H10 VH1/VK3, 5H10 VH2/VK2, 5H10 VH2/VK3 were comparable tothat of 5H10 VH0/VK0 (FIG. 11B). In agreement with Biacore data,presented above, the humanized variant 5H10 VH1/VK4 lost target binding(FIG. 11B). The isotype control did not bind to the Sl/Sl4 hSCF248cells. Based on the data presented in these studies, the humanized 2G8and 5H10 mAbs were assigned a binding score to Sl/Sl4 hSCF248 cells,which is presented in Tables 2 and 3, above.

In a separate experiment, 5H10 clones VH1/VK3, VH2/VK3, VH3/VK3,VH4/VK3, and VH5/VK3 were assessed by flow cytometry for binding to theSCF248-expressing cell line. As shown in FIGS. 11C and 11D, VH1/VK3 andVH2/VK3 exhibited high binding, maximized at 1 μg/mL. The negativecontrol was secondary antibody only. No binding was observed with thecontrol SCF220-expressing cell line (not shown).

Example 6. In Vitro Blockade of the Interaction of SCF and c-Kit

The humanized 5H10 antibodies were tested for their capacity to inhibitthe SCF-c-kit interaction and the inflammation feed-forward loop invitro. Cultured human IPF myofibroblasts (Mfb), which express surfaceSCF248, were overlaid with LAD2 mast cells, an SCF-responsive cell line.Absent any other intervention, the Mfb stimulate the LAD2 cells, whichproduce cytokines to stimulate Mfb to produce additional cytokines andextracellular matrix proteins. In this assay, the readout forinflammation and the feed-forward loop is mRNA for CCL11, collagens 1and 3, and fibronectin.

Murine 5H10 and humanized (VH1/VK3, VH2/VK3, VH3/VK3, VH4/VK3, andVH5/VK3) 5H10 antibodies were pre-incubated with Mfb at concentrationsof 1 μg/mL and 10 μg/mL to assess their capacity to inhibit thefeed-forward loop. Results are shown in FIGS. 12A-12D. The humanizedVH1/VK3 antibody consistently demonstrated inhibition of the SCF—c-kitinteraction, even at the lower concentration.

To assess the ability of humanized antibodies (5H10 VH1/VK3 and VH2/VK3)to internalize SCF248 on myofibroblasts, antibodies were labeled withpHrodo red, which is colorless at neutral pH and fluoresces red at thelow pH within an endosome. Labeled antibodies were incubated withcultured human IPF myofibroblasts for 45 minutes and red fluorescencewas visualized by microscopy. As shown in FIG. 13 , like the murineparent 5H10 antibody and the chimeric antibody (VH0/VK0), the humanizedantibodies were rapidly internalized.

Example 7. Immunogenicity of Chimeric Antibody 5H10 and Humanized LeadCandidates

The immunogenic potential of the five humanized antibodies 5H10 VH1/VK3,5H10 VH2/VK3, 5H10 VH3/VK3, 5H10 VH4/VK3, and 5H10 VH5/VK3 was comparedto the chimeric antibody 5H10 VH0/VK0.

An initial assessment of any cytotoxic effects of the samples on PBMCviability was performed for five donors used in the EpiScreen™ timecourse assays. CD8+ T cell depleted PBMC were incubated with the samplesand the viability of the cells was determined using a Luna-FL™ AutomatedCell Counter on day 7. The results showed that the mean viabilities ofPBMC from five donors treated with anti-SCF mAb were similar to that ofcells treated with medium alone, ranging between 83% and 90% (FIG. 14 ).KLH (Pierce, Life Technologies, UK) was used as a neoantigen. Exenatide(Bydueon, AstraZeneca, UK) was used as a clinical benchmark control.FIG. 15A-H and Table 6 reveal the results obtained the EpiScreen™ timecourse T cell proliferation assay of CD4+ T cell responses induced bythe samples and controls. Both the clinical benchmark, exenatide, andthe neo-antigen, KLH, elicited positive proliferative responses. A lowfrequency of positive response (SI≥1.90, p<0.05) rates were induced by5H10 VH1/VK3, 5H10 VH2/VK3, and 5H10 VH3/VK3, ranging from 4% to 8%.Sample 5H10 VH5/VK3 induced higher positive responses in 17% of thedonor cohort. 5H10 VH0/VK0 and 5H10 VH4/VK3 did not induce any positiveresponses. The mean magnitudes of the positive T cell proliferationresponses were between 2.14 and 3.61 for all samples (Table 7).

Variance analysis, ANOVA, of the whole proliferation data set (usingmaximum magnitude of proliferation between days 5-8) was used todetermine if there were any statistically significant differences in themaximum magnitude of CD4+ T cell responses to the test conditionscompared to each other and the clinical benchmark, exenatide (FIG. 16 ).The maximum magnitude of T cell proliferative responses to exenatidewere statistically higher than the responses to all the samples (Table8).

TABLE 6 Summary of healthy donor T cell proliferative responses.Positive T cell responses for proliferation (SI ≥ 1.90, p < 0.05) duringthe entire time course days 5-8 (“P”). The frequency of positiveresponses is shown as a percentage at the bottom of the columns. 5H105H10 5H10 5H10 5H10 5H10 VH0/ VH1/ VH2/ VH3/ VH4/ VH5/ Exena- VK0 VK3VK3 VK3 VK3 VK3 tide KLH Donor 1 P P Donor 2 P P Donor 3 P P Donor 4 P PP P Donor 5 P Donor 6 P P Donor 7 P Donor 8 P P Donor 9 P P Donor 10 P PDonor 11 P Donor 12 P P Donor 13 P P P Donor 14 P P P Donor 15 P P PDonor 16 P P Donor 17 P P P Donor 18 P P P Donor 19 P P Donor 20 P Donor21 P Donor 22 P P Donor 23 P Donor 24 P Proliferation 0 4 8 4 0 17 67100 %

TABLE 7 Summary of the magnitude (±SD) of positive (SI ≥ 1.90,significant p < 0.05) T cell proliferation responses. The mean SI wascalculated from the average of all positive donor responses observedduring the entire time course (days 5-8). N/A indicates not applicable.Sample Mean SI SD % Response VH0/VK0 N/A N/A 0 VH1/VK3 2.88 ±0.13 4VH2/VK3 3.61 ±1.36 8 VH3/VK3 3.09 ±0.88 4 VH4/VK3 N/A N/A 0 VH5/VK3 2.14±0.43 17 Exenatide 2.99 ±0.92 67 KLH 14.95  ±11.22 100

TABLE 8 Repeated measures one-way ANOVA (Friedman test) using a Dunn’spost-test pairs comparison. The maximum SI from the proliferation datafrom all time points of all donors were analyzed. ** p < 0.01, **** p <0.0001 and ns = not significant. 5H10 5H10 5H10 5H10 5H10 5H10 VH0/ VH1/VH2/ VH3/ VH4/ VH5/ VK0 VK3 VK3 VK3 VK3 VK3 5H10 ns VH1/VK3 5H10 ns nsVH2/VK3 5H10 ns ns ns VH3/VK3 5H10 ns ns ns ns VH4/VK3 5H10 ns ns ns nsns VH5/VK3 Exenatide **** **** **** **** **** **

In summary, the risk of clinical immunogenicity was determined bymeasuring ex vivo T cell responses using peripheral blood mononuclearcells (PBMC) isolated from 24 healthy donors representing the Europeanand North American population (based on HLA allotypes) in the EpiScreen™time course T cell assay. T cell responses were measured usingproliferation assays ([³H]-thymidine uptake). The results showed thatfour of the lead humanized antibodies had a low potential for clinicalimmunogenicity.

Example 8. Evaluation of Murine 5H10 in a Bleomycin Model of LungInflammation and Fibrosis

The bleomycin animal model of pulmonary fibrosis was employed to assessin vivo effects of 5H10. Bleomycin is a chemotherapeutic agent thatcauses pulmonary fibrosis in humans and animals. C57BL6 mice wereadministered bleomycin intratracheally on Day 1, and on Days 8 and 12received 5H10 intraperitoneally at 20 mg/kg or isotype-matched controlantibody. On Day 17 samples were collected. The 5H10-treated animals hadsignificant improvements in lung histology (FIG. 17 ), decreases in lunghydroxyproline (a quantitative measure of fibrosis; FIG. 18 ),maintenance of body weight over time (FIG. 19 ), decreases in mRNA forinflammatory cytokine and markers of myofibroblast activation (FIG. 20), and in lung mast cells, eosinophils and ILC2 lymphocytes (FIG. 21 ).Pulmonary function testing was also significantly improved (FIG. 22 ).Thus, the study demonstrated that 5H10 was effective to reduce fibrosisand inflammation, and improve pulmonary function, in an in vivo model ofpulmonary fibrosis.

Example 9. Evaluation of Humanized 5H10 Antibodies in Chronic AllergicAsthma Model

Humanized 5H10 antibodies were tested in an in vivo model of chronicallergic asthma. Mice were sensitized to cockroach antigen (CRA)intraperitoneally and subcutaneously followed by intranasal boosting ondays 14, 18, 22 and 26. On days 26, 29, 32, and 34 they wereadministered indicated humanized 5H10 antibody or PBS control,intraperitoneally at 20 mg/kg or control irrelevant antibody. On days 30and 34, they also received CRA intratracheally. On Day 35 specimens werecollected. A schematic of the study design is provided in FIG. 23 .

Airway resistance was significantly less in the animals treated withantibody 5H10 VH1/VK3 compared to PBS control as well as to otherhumanized variant antibodies (FIG. 24A). Further, in animals treatedwith VH1/VK3 or VH2/VK3, there were significant decreases in lung IL-13mRNA in relation to the chronic asthma control (i.e., compared toanimals administered CRA without any antibody treatment (PBS controls))(FIG. 24B). Moreover, matrix gene expression was significantly reducedin animals that received VH1/VK3 antibody treatment (Collagen 1 mRNAshown in FIG. 24C; Collagen 3 mRNA shown in FIG. 24D. SCF248 mRNAexpression was also significantly reduced in animals treated withVH1/VK3 (FIG. 24E). FIGS. 25A, 25B, and 25C show that VH1/VK3administration reduced mRNA levels of mucus protein Gob5 and cytokinesIL-13 and IL-5 at concentrations of 1 mg/kg and 5 mg/kg. Accordingly,the data showed that the VH1/VK3 antibody blocked cytokine and matrixgene expression in vivo in a model of chronic asthma.

Example 12. Phase 1a Clinical Trial to Evaluate Safety,Pharmacokinetics, and Pharmacodynamics of the Anti-SCF248 Antibody

A Phase 1a study will enroll 110 healthy volunteers. The primaryobjective is to obtain safety assessment and obtain accuratepharmacokinetic and pharmacodynamic data for the humanized anti-SCF248antibody 5H10.

Single and multiple ascending doses of humanized 5H10, or placebo, willbe administered, either intravenously or subcutaneously. Six to 8subjects will make up one group. The starting dose will be based ontoxicology studies performed according to good laboratory practices. Thebaseline pharmacokinetics will be obtained for all development andproduct lifetime. To assess pharmacodynamics, the number of circulatingc-kit+ cells will be assessed, including mast cell progenitor cells andtype 2 innate lymphoid (ILC2) cells, in addition to serum inflammatorymarkers such as SCF165.

Example 13. A Clinical Study to Evaluate Safety and Efficacy of theAnti-SCF248 Antibody in Patients

A clinical study will enroll patients suffering from an inflammatorydisorder such as atopic dermatitis, chronic urticaria, pulmonaryfibrosis, and/or others. One object of the study is to establish adose-response relationship between humanized 5H10 antibody andpharmacodynamic markers in diseased patients e.g. the number ofcirculating c-kit+ cells, such as mast cell progenitor cells and type 2innate lymphoid cells (ILC2) cells. Inflammatory biomarkers, such asADAMS, CCL17, EPX, RNASE3, CCL2, CCLS, tryptase, histamine and SCF165will also be measured.

A single, ascending dose of 5H10 antibody will be given to each subjectgroup. The starting dose will be based on Phase 1a pharmacodynamicbiomarkers. Patients will be treated for one, two, three, or moremonths. The results of the study will show that humanized 5H10 antibodyis effective in stabilizing and/or treating and/or preventing theprogression of inflammatory disorders and fibrotic diseases.

Publications, patents and patent applications cited herein arespecifically incorporated by reference in their entireties. While thedescribed invention has been described with reference to the specificembodiments thereof it should be understood by those skilled in the artthat various changes may be made and equivalents may be substitutedwithout departing from the true spirit and scope of the invention. Inaddition, many modifications may be made to adopt a particularsituation, material, composition of matter, process, process step orsteps, to the objective spirit and scope of the described invention. Allsuch modifications are intended to be within the scope of the claimsappended hereto.

1. An isolated nucleic acid molecule encoding an antibody or fragmentthereof that specifically binds to stem cell factor (SCF), wherein theantibody or fragment thereof comprises a heavy chain CDR1, CDR2, andCDR3 comprising SEQ ID NOs: 1, 2, and 3, respectively; and a light chainCDR1, CDR2, and CDR3 comprising SEQ ID NOs: 4, 5, and 6, respectively.2. An expression vector comprising the nucleic acid molecule of claim 1.3. A recombinant host cell comprising the expression vector of claim 2.4. A method for making an antibody or fragment thereof comprising aheavy chain CDR1, CDR2, and CDR3 comprising SEQ ID NOs: 1, 2, and 3,respectively; and a light chain CDR1, CDR2, and CDR3 comprising SEQ IDNOs: 4, 5, and 6, respectively, wherein the antibody or fragment thereofspecifically binds to stem cell factor isoform 248 (SCF248), the methodcomprising immunizing a host animal with a peptide comprising SEQ ID NO:30 or a fragment thereof, and obtaining the antibody or fragment thereoffrom the immunized host animal.
 5. The method of claim 4, wherein thepeptide comprises at least 5 amino acids and wherein the N-terminalamino acid of the peptide is the alanine at position 1 of SEQ ID NO: 30.6. A method for treating a chronic inflammatory disease or a fibroticdisease in a subject in need thereof, the method comprisingadministering to the subject an antibody or fragment thereof thatspecifically binds to stem cell factor (SCF), wherein the antibody orfragment thereof comprises a heavy chain CDR1, CDR2, and CDR3 comprisingSEQ ID NOs: 1, 2, and 3, respectively; and a light chain CDR1, CDR2, andCDR3 comprising SEQ ID NOs: 4, 5, and 6, respectively.
 7. The method ofclaim 6, wherein the chronic inflammatory disease or fibrotic disease isselected from the group consisting of urticaria, atopic dermatitis,non-alcoholic steatohepatitis (NASH), primary sclerosing cholangitis,pulmonary fibrosis, chronic obstructive pulmonary disease (COPD), acuterespiratory distress syndrome (ARDS), cystic fibrosis, peribronchialfibrosis, hypersentitivity pneumonitis, asthma, bleomycin lung,scleroderma, liver cirrhosis, endomyocardial fibrosis, fibromyalgia, andeosinophilic esophagitis.
 8. The method of claim 7, wherein the chronicinflammatory disease or fibrotic disease is pulmonary fibrosis.
 9. Themethod of claim 8, wherein the pulmonary fibrosis is idiopathicpulmonary fibrosis or scleroderma lung fibrosis.
 10. The method of claim6, wherein the method further comprises administering an additionaltherapeutic agent to the subject.
 11. A method for inhibiting theactivation of immune cells, comprising contacting the immune cells withan antibody or fragment thereof that specifically binds to stem cellfactor (SCF), wherein the antibody or fragment thereof comprises a heavychain CDR1, CDR2, and CDR3 comprising SEQ ID NOs: 1, 2, and 3,respectively; and a light chain CDR1, CDR2, and CDR3 comprising SEQ IDNOs: 4, 5, and 6, respectively.
 12. The method of claim 11, wherein theimmune cells are selected from the group consisting of mast cells,eosinophils, and innate lymphoid cells 2, and innate lymphoid cells 3.13. A method for inhibiting inflammation, fibrosis, or both in a subjectin need thereof, the method comprising administering to the subject anantibody or fragment thereof that specifically binds to stem cell factor(SCF), wherein the antibody or fragment thereof comprises a heavy chainCDR1, CDR2, and CDR3 comprising SEQ ID NOs: 1, 2, and 3, respectively;and a light chain CDR1, CDR2, and CDR3 comprising SEQ ID NOs: 4, 5, and6, respectively.
 14. A method for treating an inflammatory disease ordisorder, a fibrotic disease, or both in a subject in need thereof, themethod comprising administering to the subject an antibody or fragmentthereof that specifically binds to stem cell factor (SCF), wherein theantibody or fragment thereof comprises a heavy chain CDR1, CDR2, andCDR3 comprising SEQ ID NOs: 1, 2, and 3, respectively; and a light chainCDR1, CDR2, and CDR3 comprising SEQ ID NOs: 4, 5, and 6, respectively.15. The method of claim 14, comprising treating an inflammatory diseaseor disorder.
 16. The method of claim 15, wherein the inflammatorydisease or disorder is a chronic inflammatory disease or disorder. 17.The method of claim 14, comprising treating a fibrotic disease.
 18. Themethod of claim 14, wherein the inflammatory disease or disorder or thefibrotic disease is selected from the group consisting of urticaria,atopic dermatitis, non-alcoholic steatohepatitis (NASH), primarysclerosing cholangitis, pulmonary fibrosis, chronic obstructivepulmonary disease (COPD), acute respiratory distress syndrome (ARDS),cystic fibrosis, peribronchial fibrosis, hypersensitivity pneumonitis,asthma, bleomycin lung, scleroderma, liver cirrhosis, endomyocardialfibrosis, fibromyalgia, and eosinophilic esophagitis.
 19. A method forinhibiting chronic inflammation, fibrosis, or both in a subject in needthereof, the method comprising administering to the subject an antibodyor fragment thereof that specifically binds to stem cell factor (SCF),wherein the antibody or fragment thereof comprises a heavy chain CDR1,CDR2, and CDR3 comprising SEQ ID NOs: 1, 2, and 3, respectively; and alight chain CDR1, CDR2, and CDR3 comprising SEQ ID NOs: 4, 5, and 6,respectively.